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BPIFA1 is a secreted biomarker of differentiating human airway epithelium
In vitro culture and differentiation of human-derived airway basal cells under air-liquid interface (ALI) into a pseudostratified mucociliated mucosal barrier has proven to be a powerful preclinical tool to study pathophysiology of respiratory epithelium. As such, identifying differentiation stage-s...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9744250/ https://www.ncbi.nlm.nih.gov/pubmed/36519134 http://dx.doi.org/10.3389/fcimb.2022.1035566 |
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author | Clifton, Clarissa Niemeyer, Brian F. Novak, Richard Can, Uryan Isik Hainline, Kelly Benam, Kambez H. |
author_facet | Clifton, Clarissa Niemeyer, Brian F. Novak, Richard Can, Uryan Isik Hainline, Kelly Benam, Kambez H. |
author_sort | Clifton, Clarissa |
collection | PubMed |
description | In vitro culture and differentiation of human-derived airway basal cells under air-liquid interface (ALI) into a pseudostratified mucociliated mucosal barrier has proven to be a powerful preclinical tool to study pathophysiology of respiratory epithelium. As such, identifying differentiation stage-specific biomarkers can help investigators better characterize, standardize, and validate populations of regenerating epithelial cells prior to experimentation. Here, we applied longitudinal transcriptomic analysis and observed that the pattern and the magnitude of OMG, KRT14, STC1, BPIFA1, PLA2G7, TXNIP, S100A7 expression create a unique biosignature that robustly indicates the stage of epithelial cell differentiation. We then validated our findings by quantitative hemi-nested real-time PCR from in vitro cultures sourced from multiple donors. In addition, we demonstrated that at protein-level secretion of BPIFA1 accurately reflects the gene expression profile, with very low quantities present at the time of ALI induction but escalating levels were detectable as the epithelial cells terminally differentiated. Moreover, we observed that increase in BPIFA1 secretion closely correlates with emergence of secretory cells and an anti-inflammatory phenotype as airway epithelial cells undergo mucociliary differentiation under air-liquid interface in vitro. |
format | Online Article Text |
id | pubmed-9744250 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97442502022-12-13 BPIFA1 is a secreted biomarker of differentiating human airway epithelium Clifton, Clarissa Niemeyer, Brian F. Novak, Richard Can, Uryan Isik Hainline, Kelly Benam, Kambez H. Front Cell Infect Microbiol Cellular and Infection Microbiology In vitro culture and differentiation of human-derived airway basal cells under air-liquid interface (ALI) into a pseudostratified mucociliated mucosal barrier has proven to be a powerful preclinical tool to study pathophysiology of respiratory epithelium. As such, identifying differentiation stage-specific biomarkers can help investigators better characterize, standardize, and validate populations of regenerating epithelial cells prior to experimentation. Here, we applied longitudinal transcriptomic analysis and observed that the pattern and the magnitude of OMG, KRT14, STC1, BPIFA1, PLA2G7, TXNIP, S100A7 expression create a unique biosignature that robustly indicates the stage of epithelial cell differentiation. We then validated our findings by quantitative hemi-nested real-time PCR from in vitro cultures sourced from multiple donors. In addition, we demonstrated that at protein-level secretion of BPIFA1 accurately reflects the gene expression profile, with very low quantities present at the time of ALI induction but escalating levels were detectable as the epithelial cells terminally differentiated. Moreover, we observed that increase in BPIFA1 secretion closely correlates with emergence of secretory cells and an anti-inflammatory phenotype as airway epithelial cells undergo mucociliary differentiation under air-liquid interface in vitro. Frontiers Media S.A. 2022-11-28 /pmc/articles/PMC9744250/ /pubmed/36519134 http://dx.doi.org/10.3389/fcimb.2022.1035566 Text en Copyright © 2022 Clifton, Niemeyer, Novak, Can, Hainline and Benam https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cellular and Infection Microbiology Clifton, Clarissa Niemeyer, Brian F. Novak, Richard Can, Uryan Isik Hainline, Kelly Benam, Kambez H. BPIFA1 is a secreted biomarker of differentiating human airway epithelium |
title | BPIFA1 is a secreted biomarker of differentiating human airway epithelium |
title_full | BPIFA1 is a secreted biomarker of differentiating human airway epithelium |
title_fullStr | BPIFA1 is a secreted biomarker of differentiating human airway epithelium |
title_full_unstemmed | BPIFA1 is a secreted biomarker of differentiating human airway epithelium |
title_short | BPIFA1 is a secreted biomarker of differentiating human airway epithelium |
title_sort | bpifa1 is a secreted biomarker of differentiating human airway epithelium |
topic | Cellular and Infection Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9744250/ https://www.ncbi.nlm.nih.gov/pubmed/36519134 http://dx.doi.org/10.3389/fcimb.2022.1035566 |
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